Role of coherence and delocalization in photo-induced electron transfer at organic interfaces

被引:41
作者
Abramavicius, V. [1 ,2 ]
Pranculis, V. [2 ]
Melianas, A. [3 ]
Inganas, O. [3 ]
Gulbinas, V. [2 ]
Abramavicius, D. [1 ]
机构
[1] Vilnius Univ, Dept Theoret Phys, Fac Phys, Sauletekio 9, LT-10222 Vilnius, Lithuania
[2] Ctr Phys Sci & Technol, Savanoriu 231, LT-02300 Vilnius, Lithuania
[3] Linkoping Univ, Dept Phys Chem & Biol IFM, Biomol & Organ Elect, SE-58183 Linkoping, Sweden
关键词
CHARGE SEPARATION; GENERATION; ENERGY; STATES;
D O I
10.1038/srep32914
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photo-induced charge transfer at molecular heterojunctions has gained particular interest due to the development of organic solar cells (OSC) based on blends of electron donating and accepting materials. While charge transfer between donor and acceptor molecules can be described by Marcus theory, additional carrier delocalization and coherent propagation might play the dominant role. Here, we describe ultrafast charge separation at the interface of a conjugated polymer and an aggregate of the fullerene derivative PCBM using the stochastic Schrodinger equation (SSE) and reveal the complex time evolution of electron transfer, mediated by electronic coherence and delocalization. By fitting the model to ultrafast charge separation experiments, we estimate the extent of electron delocalization and establish the transition from coherent electron propagation to incoherent hopping. Our results indicate that even a relatively weak coupling between PCBM molecules is sufficient to facilitate electron delocalization and efficient charge separation at organic interfaces.
引用
收藏
页数:7
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